LOCATOR Overdenture Implant System 07502-02Recalls & reported problems
Zest Anchors, LLC · LOCATOR Overdenture Implant, 3.5mmD x 10mmL, 2.5mm Cuff · Class 2 · Implant
All models of LOCATOR Overdenture Implant System (74)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 17
- Deaths reported
- 0
- Injuries reported
- 17
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 17 adverse event reports that list this exact device (DI 00840481130816), received between Jan 13, 2022 and Apr 24, 2025 — classified as 17 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (15 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate15
- Loss of Osseointegration2
Patient problems
- No Clinical Signs, Symptoms or Conditions10
- Failure of Implant7
Recent adverse event reports
The 17 most recent of 17 reports, in the reporter's own words as published by the FDA.
InjuryApr 24, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 6, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 6, 2024Failure to Osseointegrate; Failure to Osseointegrate
NON-INTEGRATION. PER CUSTOMER, IMPLANT FAILED TO TAKE DURING PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20865236 ↗InjuryDec 6, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 25, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 29, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF INTEGRATION..
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19418442 ↗InjuryMay 29, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 16, 2023Failure to Osseointegrate; Failure to Osseointegrate
FAILURE TO INTEGRATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16388323 ↗InjuryFeb 16, 2023Failure to Osseointegrate; Failure to Osseointegrate
FAILURE TO INTEGRATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16387818 ↗InjuryJan 10, 2023Loss of Osseointegration; Loss of Osseointegration
IMPLANT LOST INTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16134733 ↗InjuryMay 9, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 9, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 18, 2022Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT FAILED TO INTEGRATE. NON INTEGRATION.
Patient problems: Failure of Implant
MAUDE report 13804236 ↗InjuryFeb 10, 2022Failure to Osseointegrate; Failure to Osseointegrate
IT WAS REPORTED THAT THE IMPLANT FAILED TO INTEGRATE AND WAS REMOVED.
Patient problems: Failure of Implant
MAUDE report 13506825 ↗InjuryFeb 1, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 19, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 13, 2022Failure to Osseointegrate; Failure to Osseointegrate
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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